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Reprocessed Micro Sagittal Blade, Fine, 5.5 x 18.5 x 0.4mm

FDA UDI

Class I (US FDA UDI)

by Suretek Medical

Identity

Trade Name
Reprocessed Micro Sagittal Blade, Fine, 5.5 x 18.5 x 0.4mm FDA UDI
Generic Name
Surgical saw blade, sagittal, reprocessed FDA UDI
Model / Reference
5023-144 FDA UDI

Identifiers

Primary DI / UDI-DI
B39050231441 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, sagittal, reprocessed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical saw blade, sagittal, reprocessed

A medical device review directory listing the Reprocessed Micro Sagittal Blade, Fine, 5.5 x 18.5 x 0.4mm surgical saw blade for orthopaedic or oral surgery, designed with a flat cutting instrument made of high-grade stainless steel and serrated edge attached to a dedicated powered saw. This previously used single-use device has been reprocessed for an additional patient application.

Similar devices

Also classified as Surgical saw blade, sagittal, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Suretek Medical

Sources (1)

  • FDA UDI 0039eae0-cf56-422f-a04b-8cc432ad7e5f 32 fields · synced Jun 27, 2026